University of California San Francisco Comprehensive Cancer Center, San Francisco, California, USA.
Pfizer Inc., New York, New York, USA.
Int J Cancer. 2024 Feb 15;154(4):701-711. doi: 10.1002/ijc.34748. Epub 2023 Oct 13.
There are limited real-world comparative effectiveness data for palbociclib plus an aromatase inhibitor (AI) as a first-line (1L) treatment examining endpoints that require long term follow-up and post 1L progression. The Flatiron Health Analytic Database was used to characterize treatment and dosing patterns in patients with hormone receptor-positive/human epidermal growth factor 2-negative (HR+/HER2-) metastatic breast cancer (mBC) receiving palbociclib plus an AI vs an AI alone in routine US clinical practice. In addition, time to chemotherapy (TTC) and real-world progression-free survival (rwPFS) when combining 1L and second-line of therapy (rwPFS2) were assessed. Of 1324 patients who received palbociclib plus an AI between February 3, 2015 and March 31, 2020, 1110 (83.8%) started palbociclib at the recommended 125 mg/day dose. After stabilized inverse probability treatment-weighting (sIPTW), median TTC in patients treated with palbociclib plus an AI and AI alone was 37.4 months (95% confidence interval [CI], 33.7-40.7) and 29.2 months (95% CI, 26.8-33.5), respectively (hazard ratio [HR] = 0.77 [95% CI, 0.69-0.86], P < .0001); median rwPFS2 was 32.6 months (95% CI, 29.4-35.2) and 20.7 months (95% CI, 18.9-22.6), respectively (HR = 0.62 [95% CI, 0.54-0.70], P < .0001). Sensitivity analyses with propensity score matching showed similar results to sIPTW analyses. Results from this large real-world study examining additional effectiveness outcomes beyond 1L rwPFS and overall survival support the use of palbociclib plus an AI as a 1L treatment for patients with HR+/HER2- mBC.
在需要长期随访和一线治疗进展后评估的终点方面,帕博西利联合芳香化酶抑制剂(AI)作为一线(1L)治疗的真实世界比较疗效数据有限。使用 Flatiron Health 分析数据库描述了在常规美国临床实践中,接受帕博西利联合 AI 与单独 AI 治疗的激素受体阳性/人表皮生长因子受体 2 阴性(HR+/HER2-)转移性乳腺癌(mBC)患者的治疗和剂量模式。此外,评估了 1L 和二线治疗(rwPFS2)联合的化疗开始时间(TTC)和真实世界无进展生存期(rwPFS)。在 2015 年 2 月 3 日至 2020 年 3 月 31 日期间接受帕博西利联合 AI 治疗的 1324 例患者中,有 1110 例(83.8%)以推荐的 125mg/天剂量开始使用帕博西利。经过稳定的逆概率治疗加权(sIPTW)后,接受帕博西利联合 AI 和单独 AI 治疗的患者的中位 TTC 分别为 37.4 个月(95%置信区间 [CI],33.7-40.7)和 29.2 个月(95% CI,26.8-33.5)(风险比 [HR] = 0.77 [95% CI,0.69-0.86],P<0.0001);中位 rwPFS2 分别为 32.6 个月(95% CI,29.4-35.2)和 20.7 个月(95% CI,18.9-22.6)(HR = 0.62 [95% CI,0.54-0.70],P<0.0001)。倾向性评分匹配的敏感性分析结果与 sIPTW 分析相似。这项大型真实世界研究的结果表明,除了 1L rwPFS 和总生存期之外,还观察到了其他疗效终点,支持将帕博西利联合 AI 作为 HR+/HER2-mBC 患者的一线治疗。